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通过化学蚀刻 pH 敏感的聚集诱导发射活性金纳米团簇,用于半胱氨酸的超灵敏检测。

Chemical etching of pH-sensitive aggregation-induced emission-active gold nanoclusters for ultra-sensitive detection of cysteine.

机构信息

Beijing Advanced Innovation Center for Materials Genome Engineering, Research Center for Bioengineering and Sensing Technology, School of Chemistry and Biological Engineering, University of Science and Technology Beijing, Beijing 100083, P. R. China.

出版信息

Nanoscale. 2018 Dec 20;11(1):294-300. doi: 10.1039/c8nr08526a.

Abstract

This study reports the utilization of thiol-induced chemical etching of aggregation-induced emission (AIE)-active Au nanoclusters (NCs) for the facile, sensitive, and selective detection of cysteine. The AIE-active Au NCs were formed in an acidic solution containing excess Au(i)-thiolate complexes. At an acidic pH (2.0), the emission of these Au NCs was enhanced by cysteine at a concentratioin below 1 mM. However, the emission was quenched by cysteine at a high concentration, e.g., 500 mM, via the thiol-induced etching of gold, although the process occurred very slowly. Interestingly, in the absence of cysteine, increasing the solution pH enhanced the emission, while the presence of cysteine remarkably accelerated the etching-induced quenching process. The complete quenching of the emission by excess cysteine at pH 2.0 and the enhancement of the emission by the increasing pH in the absence of cysteine indicated that aurophilicity might not be involved in the AIE of the Au NCs prepared using glutathione (GSH) both as the reducing and protecting reagent. On the other hand, the etching process involved the penetration of cysteine molecules through the Au(i)-thiolate complexes, which could assemble or disassemble around the embedded Au NCs in response to the solution pH to get access to the innermost Au(0) cores. Therefore, a facile, sensitive, and selective method for the detection of cysteine was established. This method exhibited an extremely wide linear range as wide as nine orders of magnitude above the cysteine concentration, including two linear regions of the relative emission intensity of the Au NCs versus the logarithm of cysteine concentration, from 10 pM to 150 μM (correlation coefficient, 0.99851) and from 150 μM to 2 mM (correlation coefficient, 0.99866). An ultra-low limit of detection of 6.3 pM (S/N = 3) was also achieved. The developed method showed superior selectivity for cysteine relative to the 19 other natural amino acids and GSH. The method was applied for the analysis of human serum samples spiked with cysteine with satisfactory results. This study demonstrates the potential of the thiol-induced chemical etching approach as a powerful tool for studying luminescent metal NCs.

摘要

本研究报告了利用巯基诱导的聚集诱导发光(AIE)活性金纳米簇(NCs)的化学蚀刻,用于简便、灵敏和选择性地检测半胱氨酸。在含有过量 Au(i)-硫醇配合物的酸性溶液中形成 AIE 活性 Au NCs。在酸性 pH(2.0)下,低于 1 mM 的半胱氨酸浓度对半胱氨酸的发光有增强作用。然而,半胱氨酸的高浓度(例如 500 mM)通过金的巯基诱导蚀刻使发光猝灭,尽管该过程发生得非常缓慢。有趣的是,在没有半胱氨酸的情况下,增加溶液 pH 会增强发射,而在没有半胱氨酸的情况下,存在半胱氨酸会显著加速蚀刻诱导的猝灭过程。在 pH 2.0 下,过量半胱氨酸完全猝灭发射,而在没有半胱氨酸的情况下,随着 pH 的增加,发射增强,这表明金纳米簇的 AIE 可能不涉及使用谷胱甘肽(GSH)作为还原剂和保护剂制备的金纳米簇的金亲合性。另一方面,蚀刻过程涉及半胱氨酸分子通过 Au(i)-硫醇配合物的渗透,该配合物可以在响应溶液 pH 的情况下组装或解组装围绕嵌入的 Au NCs,以进入最内层的 Au(0)核。因此,建立了一种简便、灵敏和选择性检测半胱氨酸的方法。该方法表现出非常宽的线性范围,其半胱氨酸浓度高达九个数量级,包括金纳米簇的相对发射强度与半胱氨酸浓度对数的两个线性区域,从 10 pM 到 150 μM(相关系数,0.99851)和从 150 μM 到 2 mM(相关系数,0.99866)。检测限也低至 6.3 pM(S/N = 3)。与其他 19 种天然氨基酸和 GSH 相比,该方法对半胱氨酸具有优越的选择性。该方法用于分析人血清样品中添加的半胱氨酸,结果令人满意。本研究证明了巯基诱导的化学蚀刻方法作为研究发光金属 NCs 的有力工具的潜力。

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